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UA58502C2 - ЗАМІЩЕНІ ПОХІДНІ 4-ГІДРОКСИ-ФЕНІЛАЛКАНОЇНОВОЇ КИСЛОТИ КОНКУРЕНТНОЇ ДІЇ ДО АППР-<font face="Symbol">g,</font> ФАРМАЦЕВТИЧНА КОМПОЗИЦІЯ, СПОСІБ ЛІКУВАННЯ АБО ПОПЕРЕДЖЕННЯ ЗАХВОРЮВАНЬ, СПОСІБ ЗНИЖЕННЯ РІВНЯ ГЛЮКОЗИ У КРОВІ ТА СПОСІБ ОДЕРЖАННЯ ПОХІДНИХ - Google Patents

ЗАМІЩЕНІ ПОХІДНІ 4-ГІДРОКСИ-ФЕНІЛАЛКАНОЇНОВОЇ КИСЛОТИ КОНКУРЕНТНОЇ ДІЇ ДО АППР-<font face="Symbol">g,</font> ФАРМАЦЕВТИЧНА КОМПОЗИЦІЯ, СПОСІБ ЛІКУВАННЯ АБО ПОПЕРЕДЖЕННЯ ЗАХВОРЮВАНЬ, СПОСІБ ЗНИЖЕННЯ РІВНЯ ГЛЮКОЗИ У КРОВІ ТА СПОСІБ ОДЕРЖАННЯ ПОХІДНИХ Download PDF

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Publication number
UA58502C2
UA58502C2 UA98084544A UA98084544A UA58502C2 UA 58502 C2 UA58502 C2 UA 58502C2 UA 98084544 A UA98084544 A UA 98084544A UA 98084544 A UA98084544 A UA 98084544A UA 58502 C2 UA58502 C2 UA 58502C2
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UA
Ukraine
Prior art keywords
phenyl
mmol
alkyl
methyl
ethoxy
Prior art date
Application number
UA98084544A
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English (en)
Russian (ru)
Ukrainian (uk)
Inventor
Тімоті Марк Віллсон
молодший Мук Роберт Ентоні
Іштван Калдор
Бред Річард Хенке
Дейвід Норман Дітон
Джон Лорен Коллінз
Джефрі Едмонд Кобб
Маркус Бракін
Метью Джуд Шарп
Джон Марк О'Келлеген
Ґреґ Алан Еріксон
Ґрейді Еван Бозвелл
Original Assignee
Глаксо Груп Лімітед
Глаксо Груп Лимитед
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=10789571&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=UA58502(C2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Глаксо Груп Лімітед, Глаксо Груп Лимитед filed Critical Глаксо Груп Лімітед
Publication of UA58502C2 publication Critical patent/UA58502C2/uk

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    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D213/63One oxygen atom
    • C07D213/64One oxygen atom attached in position 2 or 6
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    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/192Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid 
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    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
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UA98084544A 1996-02-28 1997-02-26 ЗАМІЩЕНІ ПОХІДНІ 4-ГІДРОКСИ-ФЕНІЛАЛКАНОЇНОВОЇ КИСЛОТИ КОНКУРЕНТНОЇ ДІЇ ДО АППР-<font face="Symbol">g,</font> ФАРМАЦЕВТИЧНА КОМПОЗИЦІЯ, СПОСІБ ЛІКУВАННЯ АБО ПОПЕРЕДЖЕННЯ ЗАХВОРЮВАНЬ, СПОСІБ ЗНИЖЕННЯ РІВНЯ ГЛЮКОЗИ У КРОВІ ТА СПОСІБ ОДЕРЖАННЯ ПОХІДНИХ UA58502C2 (uk)

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Families Citing this family (175)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3215048B2 (ja) 1996-04-03 2001-10-02 日本たばこ産業株式会社 プロピオン酸誘導体及びその用途
CA2259487A1 (fr) 1996-07-01 1998-01-08 Margaret Mary Faul Composes hypoglycemiants et hypolipidemiants
EE03765B1 (et) * 1996-08-19 2002-06-17 Japan Tobacco Inc. Propioonhappe derivaadid ja nende kasutamine
CA2323889A1 (fr) 1997-03-12 1998-09-17 Robert W. Esmond Procede de traitement ou de prevention de la maladie d'alzheimer
EP0903343B1 (fr) * 1997-09-19 2003-05-28 SSP Co., Ltd. Dérivés d'acide phénylpropionique substitué en alfa et médicament le contenant
CA2305808A1 (fr) * 1997-10-02 1999-04-15 Sankyo Company Limited Derives d'acide amidocarboxylique
US6444816B1 (en) * 1997-10-27 2002-09-03 Dr. Reddy's Research Foundation Fused 7-oxo-pyrimidinyl compounds, preparation, composition and use thereof
US6329372B1 (en) * 1998-01-27 2001-12-11 Celltech Therapeutics Limited Phenylalanine derivatives
WO1999038845A1 (fr) 1998-01-29 1999-08-05 Tularik Inc. MODULATEURS DU RECEPTEUR ACTIVE DE LA PROLIFERATION DES PEROXYSOMES (PPARη)
US6583157B2 (en) 1998-01-29 2003-06-24 Tularik Inc. Quinolinyl and benzothiazolyl modulators
WO1999043642A1 (fr) 1998-02-26 1999-09-02 Celltech Therapeutics Limited Derives de phenylalanine en tant qu'inhibiteurs d'integrines alpha 4
GB9805655D0 (en) 1998-03-16 1998-05-13 Celltech Therapeutics Ltd Chemical compounds
US6521626B1 (en) 1998-03-24 2003-02-18 Celltech R&D Limited Thiocarboxamide derivatives
BR9910371A (pt) 1998-05-11 2001-01-09 Takera Chemical Ind Ltd Composto, composição farmacêutica, agente para controlar os receptores relacionados com a retinóide, processos de prevenção e terapia da diabetes mellitus, de prevenção e terapia da hiperlipemia, para acentuar uma sensibilidade à insulina, para melhorar uma resistência à insulina, de prevenção e terapia da tolerância à glicose prejudicada, de prevenção e terapia de uma doença inflamatória, de prevenção de uma esclerose arterial, e, uso do composto
GB9811159D0 (en) 1998-05-22 1998-07-22 Celltech Therapeutics Ltd Chemical compounds
GB9811969D0 (en) 1998-06-03 1998-07-29 Celltech Therapeutics Ltd Chemical compounds
SE9801992D0 (sv) 1998-06-04 1998-06-04 Astra Ab New 3-aryl-2-hydroxypropionic acid derivative I
MA26634A1 (fr) * 1998-06-04 2004-12-20 Astra Ab Nouveaux derives de l'acide 3-aryl propionique et analogues
RU2243214C2 (ru) * 1998-06-04 2004-12-27 Астразенека Аб Новые производные и аналоги 3-арилпропионовой кислоты
SE9801990D0 (sv) * 1998-06-04 1998-06-04 Astra Ab New 3-aryl propionic acid derivatives and analogs
US7045519B2 (en) 1998-06-19 2006-05-16 Chiron Corporation Inhibitors of glycogen synthase kinase 3
ATE274510T1 (de) * 1998-06-19 2004-09-15 Chiron Corp Glycogen synthase kinase 3 inhibitoren
GB9814414D0 (en) 1998-07-03 1998-09-02 Celltech Therapeutics Ltd Chemical compounds
GB9817118D0 (en) * 1998-08-07 1998-10-07 Glaxo Group Ltd Pharmaceutical compounds
GB9821061D0 (en) * 1998-09-28 1998-11-18 Celltech Therapeutics Ltd Chemical compounds
GB9821222D0 (en) 1998-09-30 1998-11-25 Celltech Therapeutics Ltd Chemical compounds
US6589969B1 (en) * 1998-10-16 2003-07-08 Ono Pharmaceutical Co., Ltd. Carboxylic acid derivatives and drugs containing the same as the active ingredient
GB9825652D0 (en) 1998-11-23 1999-01-13 Celltech Therapeutics Ltd Chemical compounds
GB9826174D0 (en) 1998-11-30 1999-01-20 Celltech Therapeutics Ltd Chemical compounds
CA2355645A1 (fr) * 1998-12-17 2000-06-22 Mindset Biopharmaceuticals (Usa), Inc. Utilisation accrue de glucose par le cerveau
US6204288B1 (en) 1999-03-08 2001-03-20 The University Of Mississippi 1,2-dithiolane derivatives
US6127394A (en) * 1999-03-08 2000-10-03 The University Of Mississippi 1,2-Dithiolane derivatives
AU760163B2 (en) * 1999-04-06 2003-05-08 Sankyo Company Limited Alpha-substituted carboxylic acid derivatives
MXPA01010472A (es) * 1999-04-16 2002-05-06 Reddy Research Foundation Formas polimorficas novedosas de un agente contra la diabetes; procedimiento para su preparacion y composiciones farmaceuticas que las contienen.
AU3957800A (en) * 1999-04-16 2000-11-02 Dr. Reddy's Research Foundation Crystalline r- guanidines, arginine or (l) -arginine (2(s)) -2- ethoxy -3-(4- (2-(10(h) -phenoxazin -10-yl)ethoxy}phenyl)propanoate
US6528507B1 (en) 1999-04-16 2003-03-04 Dr. Reddy's Laboratories Limited Polymorphic forms of an antidiabetic agent: process for their preparation and a pharmaceutical composition containing them
JP2002542224A (ja) * 1999-04-19 2002-12-10 コーエラカント コーポレイション Ii型糖尿病の治療薬としてのppar−(ガンマ)作用物質
US7414128B2 (en) 1999-04-20 2008-08-19 Dr. Reddy's Laboratories, Limited Crystalline R-guanidines, Arginine or (L)-Arginine (2S)-2-Ethoxy-3-{4-[2-(10H -phenoxazin-10-yl)ethoxy]phenyl}propanoate
JP2002542246A (ja) * 1999-04-20 2002-12-10 ノボ ノルディスク アクティーゼルスカブ 新規な化合物、それらの製造及び使用
WO2000063190A1 (fr) * 1999-04-20 2000-10-26 Novo Nordisk A/S Nouveaux composes, leur preparation et utilisation
US6972294B1 (en) 1999-04-20 2005-12-06 Novo Nordisk, A/S Compounds, their preparation and use
US6369055B1 (en) 1999-04-20 2002-04-09 Novo Nordisk A/S Compounds, their preparation and use
US6274608B1 (en) 1999-04-20 2001-08-14 Novo Nordisk A/S Compounds, their preparation and use
BR0009864A (pt) * 1999-04-20 2002-01-08 Novo Nordisk As Composto, composição farmacêutica, métodos para o tratamento de doenças, para o tratamento e/ou prevenção de condições mediadas pelos receptores nucleares e para o tratamento e/ou prevenção de diabete e/ou obesidade, e, uso de um composto
HUP0600105A3 (en) * 1999-04-28 2006-11-28 Reddys Lab Ltd Dr Substituted benzocondensated heterocycles, process for their preparation and their use as antiobesity and hypocholesterolemic agents
DE60027420T2 (de) * 1999-04-28 2006-11-16 Aventis Pharma Deutschland Gmbh Tri-aryl-säurederivate als ppar rezeptor liganden
US6518283B1 (en) 1999-05-28 2003-02-11 Celltech R&D Limited Squaric acid derivatives
JP4618845B2 (ja) * 1999-06-09 2011-01-26 杏林製薬株式会社 ヒトペルオキシゾーム増殖薬活性化受容体(PPAR)αアゴニストとしての置換フェニルプロピオン酸誘導体
GB9913782D0 (en) * 1999-06-14 1999-08-11 Smithkline Beecham Plc Novel compounds
GB9914977D0 (en) * 1999-06-25 1999-08-25 Glaxo Group Ltd Chemical compounds
JP4295458B2 (ja) * 1999-06-30 2009-07-15 アムジェン インコーポレイテッド Ppar−ガンマ活性調節用化合物
US7041691B1 (en) 1999-06-30 2006-05-09 Amgen Inc. Compounds for the modulation of PPARγ activity
CA2382966A1 (fr) 1999-08-27 2001-03-08 Eli Lilly And Company Derives de biaryl-oxa(thia)zole et leur utilisation en tant que modulateurs de ppar
AU778282B2 (en) * 1999-09-17 2004-11-25 Kyorin Pharmaceutical Co. Ltd. O-anisamide derivatives
US6414002B1 (en) 1999-09-22 2002-07-02 Bristol-Myers Squibb Company Substituted acid derivatives useful as antidiabetic and antiobesity agents and method
EP1939188A1 (fr) * 1999-09-22 2008-07-02 Bristol-Myers Squibb Company Dérivés d'oxa et thiazole utiles en tant qu'agents antidiabétiques et anti-obésité
TWI302149B (en) * 1999-09-22 2008-10-21 Bristol Myers Squibb Co Substituted acid derivatives useful as antiodiabetic and antiobesity agents and method
US6534513B1 (en) 1999-09-29 2003-03-18 Celltech R&D Limited Phenylalkanoic acid derivatives
SE9904415D0 (sv) * 1999-12-03 1999-12-03 Astra Ab New process
CA2393265A1 (fr) * 1999-12-03 2001-06-07 Kyoto Pharmaceutical Industries, Ltd. Nouveaux composes heterocycliques et sels de ces derniers, utilisations de ces composes en medecine
PT1237855E (pt) * 1999-12-03 2004-06-30 Astrazeneca Ab Forma cristalina do acido (s)-2-etoxi-3-¬4-(2-{4-metanosulfoniloxifenil}etoxi)fenil|propanoico
SE9904413D0 (sv) * 1999-12-03 1999-12-03 Astra Ab Comminuted form
US6455539B2 (en) 1999-12-23 2002-09-24 Celltech R&D Limited Squaric acid derivates
JP4316787B2 (ja) * 2000-01-11 2009-08-19 壽製薬株式会社 エーテル又はアミド誘導体、その製法並びにそれを含有する糖尿病治療剤、
JP2001261674A (ja) * 2000-03-22 2001-09-26 Mitsui Chemicals Inc ベンゾチオフェン誘導体およびそれを有効成分として含有する核内レセプター作動薬
JP2003531141A (ja) 2000-04-17 2003-10-21 セルテック アール アンド ディ リミテッド エナミン誘導体
US6653332B2 (en) 2000-05-03 2003-11-25 Tularik Inc. Combination therapeutic compositions and method of use
FR2808798A1 (fr) * 2000-05-09 2001-11-16 Hoechst Marion Roussel Inc Nouveaux derives antagonistes du recepteur de la vitronectine
US6545013B2 (en) 2000-05-30 2003-04-08 Celltech R&D Limited 2,7-naphthyridine derivatives
US6403608B1 (en) 2000-05-30 2002-06-11 Celltech R&D, Ltd. 3-Substituted isoquinolin-1-yl derivatives
GB0014969D0 (en) 2000-06-19 2000-08-09 Smithkline Beecham Plc Novel method of treatment
US20030171399A1 (en) 2000-06-28 2003-09-11 Tularik Inc. Quinolinyl and benzothiazolyl modulators
WO2002004426A1 (fr) 2000-07-07 2002-01-17 Celltech R & D Limited Derives d'acide squarique contenant un noyau heteroaromatique bicyclique comme antagonistes d'integrine
JP2004505110A (ja) 2000-08-02 2004-02-19 セルテック アール アンド ディ リミテッド 3位置換イソキノリン−1−イル誘導体
AU2001278738A1 (en) * 2000-08-16 2002-02-25 Sankyo Company Limited Medicinal compositions for preventing and treating cancer
CN1471517A (zh) 2000-08-23 2004-01-28 Cxazolyl-芳基丙酸衍生物及其作为过氧化物酶体增殖物活化受体激动剂的用途
AU2001284658A1 (en) 2000-08-23 2002-03-13 Eli Lilly And Company Oxazolyl-aryloxyacetic acid derivatives and their use as ppar agonists
CA2418134A1 (fr) 2000-08-23 2002-02-28 Eli Lilly And Company Derives d'acide oxazolyl-arylpropionique et leur utilisation comme agonistes des ppar
GB0030845D0 (en) * 2000-12-18 2001-01-31 Smithkline Beecham Plc Novel treatment
US6982251B2 (en) 2000-12-20 2006-01-03 Schering Corporation Substituted 2-azetidinones useful as hypocholesterolemic agents
CN100357280C (zh) * 2000-12-25 2007-12-26 小野药品工业株式会社 二氢化萘衍生物及包含该衍生物作为活性成分的药物
EP1695716A2 (fr) 2000-12-26 2006-08-30 Sankyo Company, Limited Compositions médicinales contenant un diuretique et un agent renforcant la résistance a l'insuline
US7071181B2 (en) 2001-01-26 2006-07-04 Schering Corporation Methods and therapeutic combinations for the treatment of diabetes using sterol absorption inhibitors
ATE331512T1 (de) 2001-01-26 2006-07-15 Schering Corp Verwendung azetidinone-substituierter verbindungen zur behandlung der sitosterolhämie
MEP27808A (en) 2001-01-26 2010-10-10 Schering Corp Combinations of peroxisome proliferator-activated receptor (ppar) activator(s) and sterol absorption inhibitor(s) and treatments for vascular indications
EP1911462A3 (fr) 2001-01-26 2011-11-30 Schering Corporation Combinaisons comprenant un inhibiteur d'absorption de stérol
US7138390B2 (en) 2001-03-12 2006-11-21 Intercept Pharmaceuticals Steroids as agonists for FXR
ATE480236T1 (de) * 2001-04-25 2010-09-15 Takeda Pharmaceutical Verwendung des abc-expressionspromotors pioglitazon zur behandlung von arteriosklerose obliterans
MXPA03010435A (es) * 2001-05-15 2004-03-09 Hoffmann La Roche Derivados de oxazol acido carboxilico sustituidos para uso como activadores de proliferacion del peroximosa(ppar-alfa y gama) en el tratamiento de diabetes.
RU2287529C2 (ru) 2001-05-29 2006-11-20 Киото Фармасьютикал Индастриз, Лтд. Новые гетероциклические производные и их медицинское использование
MXPA03010811A (es) 2001-05-29 2004-02-27 Kyoto Pharma Ind Compuestos heterociclico y uso farmaceutico.
DE10127126A1 (de) * 2001-06-05 2002-12-19 Forschungszentrum Juelich Gmbh Geschützte Tyrosinderivate, Verfahren zu deren Herstellung und deren Verwendung zur Herstellung von O-(2-[·18·F]-Fluorethyl)-L-tyrosin
CA2449256A1 (fr) * 2001-06-07 2002-12-19 Eli Lilly And Company Modulateurs de recepteurs actives par le proliferateur de peroxysome
EA200400011A1 (ru) 2001-06-07 2004-06-24 Эли Лилли Энд Компани Модуляторы рецепторов, активируемых пролифераторами пероксисом (prar)
WO2003011814A1 (fr) * 2001-07-30 2003-02-13 Novo Nordisk A/S Nouveaux derives de vinyl n-(2-benzoylphenyl)-l-tyrosine et leur utilisation en tant qu'agents antidiabetiques, etc.
US7067530B2 (en) 2001-07-30 2006-06-27 Novo Nordisk A/S Compounds, their preparation and use
EP1414806A1 (fr) * 2001-07-30 2004-05-06 Novo Nordisk A/S Nouveaux derives de vinyl n-(2-benzoylphenyl)-l-tyrosine et leur utilisation en tant qu'antidiabetiques etc.
US20030171377A1 (en) * 2001-08-29 2003-09-11 Bigge Christopher Franklin Antidiabetic agents
US7053080B2 (en) 2001-09-21 2006-05-30 Schering Corporation Methods and therapeutic combinations for the treatment of obesity using sterol absorption inhibitors
US7056906B2 (en) 2001-09-21 2006-06-06 Schering Corporation Combinations of hormone replacement therapy composition(s) and sterol absorption inhibitor(s) and treatments for vascular conditions in post-menopausal women
JP2005504091A (ja) 2001-09-21 2005-02-10 シェーリング コーポレイション ステロール吸収阻害剤としてアゼチジノンを用いる黄色腫の処置
TW200300681A (en) 2001-11-12 2003-06-16 Ono Pharmaceutical Co Carboxylic acid derivative compound and medicament containing same as active ingredient
HUP0402486A3 (en) * 2001-11-30 2007-05-02 Lilly Co Eli Nitrogen containing heterocyclic compounds as peroxisome proliferator activated receptor agonists, their use and pharmaceutical compositions cointaining them
AU2002354460A1 (en) * 2001-12-11 2003-07-09 Sankyo Company, Limited Medicinal composition
DE60209824T2 (de) * 2001-12-21 2006-10-19 Smithkline Beecham Corp. Dosierschema für ppar-gamma-aktivatoren
AU2002366980A1 (en) 2002-01-17 2003-07-30 Toaeiyo Ltd. Halogenobenzyl aminopropionic acid derivatives
JPWO2003062427A1 (ja) * 2002-01-23 2005-05-26 山之内製薬株式会社 インスリン抵抗性改善薬のスクリーニング法
US6716842B2 (en) 2002-04-05 2004-04-06 Warner-Lambert Company, Llc Antidiabetic agents
JP2004277397A (ja) * 2002-05-24 2004-10-07 Takeda Chem Ind Ltd 1,2−アゾール誘導体
AU2003241173A1 (en) * 2002-05-24 2003-12-12 Takeda Pharmaceutical Company Limited 1,2-azole derivatives with hypoglycemic and hypolipidemic activity
GB0214149D0 (en) * 2002-06-19 2002-07-31 Glaxo Group Ltd Chemical compounds
AU2003259131A1 (en) 2002-07-09 2004-01-23 Bristol-Myers Squibb Company Substituted heterocyclic derivatives useful as antidiabetic and antiobesity agents and method
NZ537251A (en) 2002-07-09 2007-02-23 Bristol Myers Squibb Co Substituted heterocyclic derivatives useful as antidiabetic and antiobesity agents and method
AR041481A1 (es) * 2002-10-07 2005-05-18 Hoffmann La Roche Derivados de acido arilpropionico-oxazol y su uso como agonistas de ppar
WO2004037248A2 (fr) * 2002-10-24 2004-05-06 Carex Sa Modulation de l'activite des recepteurs actives par les proliferateurs de peroxysomes
WO2004043457A1 (fr) 2002-11-06 2004-05-27 Schering Corporation Inhibiteurs d'absorption de cholesterol pour le traitement de troubles auto-immuns
US7960369B2 (en) 2002-11-08 2011-06-14 Takeda Pharmaceutical Company Limited Receptor function regulator
KR100699614B1 (ko) * 2002-11-08 2007-03-23 에프. 호프만-라 로슈 아게 퍼옥시좀 증식자 활성화된 수용체 작용제로서의 치환된4-알콕시옥사졸 유도체
US7268157B2 (en) * 2002-11-26 2007-09-11 Shenzhen Chipscreen Biosciences, Ltd. Substituted arylalcanoic acid derivatives as PPAR pan agonists with potent antihyperglycemic and antihyperlipidemic activity
US6653334B1 (en) 2002-12-27 2003-11-25 Kowa Co., Ltd. Benzoxazole compound and pharmaceutical composition containing the same
BRPI0407180A (pt) 2003-02-14 2006-02-07 Lilly Co Eli Composto, composição farmacêutica, métodos para modular um receptor ativado pelo proliferador de peroxissoma, para tratar ou prevenir uma doença ou condição, para diminuir a glicose no sangue em um mamìfero, para tratar ou prevenir diabetes mellitus, doença cardiovascular e sìndrome x em um mamìfero, e, uso de um composto
GB0303600D0 (en) * 2003-02-17 2003-03-19 Glaxo Group Ltd Novel therapeutic method and compositions
US20060142356A1 (en) * 2003-02-17 2006-06-29 Davis Adrian F Novel therapeutic method and compositions for topical administration
MXPA05009501A (es) 2003-03-07 2005-10-18 Schering Corp Compuestos de azetidinona sustituidos, formulaciones y usos de los mismos para el tratamiento de hipercolesterolemia.
US7459442B2 (en) 2003-03-07 2008-12-02 Schering Corporation Substituted azetidinone compounds, processes for preparing the same, formulations and uses thereof
EP1606287B1 (fr) 2003-03-07 2013-10-02 Merck Sharp & Dohme Corp. Composés d'azetidinone substitués, formulations et utilisations de ceux-ci pour traiter l'hypercholestérolémie
CA2517571C (fr) 2003-03-07 2011-07-05 Schering Corporation Azetidinones substituees , procedes pour leur preparation, formulations et utilisations de celles-ci
CN1812988A (zh) * 2003-05-13 2006-08-02 斯索恩有限公司 制备噻唑烷二酮衍生物的方法及其化合物
CA2530452C (fr) 2003-07-02 2011-07-26 F. Hoffmann-La Roche Ag Derives d'indolyle substitues par un cycle thiazole et leur utilisation comme modulateurs de ppar
EP1658273B1 (fr) * 2003-08-20 2007-01-03 Eli Lilly And Company Composes, procedes et preparations destines a l'apport oral d'un compose peptidique de type glucagon (glp-1) ou d'un peptide agoniste du recepteur 4 de melanocortine (mc4)
ATE361294T1 (de) * 2003-08-20 2007-05-15 Lilly Co Eli Verbindungen, verfahren und formulierungen zur oralen verabreichung einer glucagonartigen peptid (glp)-1-verbindung oder eines melanocortin-4- rezeptor-(mc4-)agonistschen peptids
US7223761B2 (en) 2003-10-03 2007-05-29 Amgen Inc. Salts and polymorphs of a potent antidiabetic compound
TW200526588A (en) * 2003-11-17 2005-08-16 Smithkline Beecham Corp Chemical compounds
US8008525B2 (en) 2003-11-26 2011-08-30 Takeda Pharmaceutical Company Limited Receptor function regulating agent
MXPA06006829A (es) * 2003-12-15 2006-08-23 Lilly Co Eli Moduladores del receptor activado por el proliferador selectivo de peroxisoma.
TW200523247A (en) 2003-12-25 2005-07-16 Takeda Pharmaceutical 3-(4-benzyloxyphenyl) propanoic acid derivatives
US7585880B2 (en) 2003-12-26 2009-09-08 Takeda Pharmaceutical Company Limited Phenylpropanoic acid derivatives
AU2005219536A1 (en) * 2004-03-09 2005-09-15 F. Hoffmann-La Roche Ag Pyrazolyl indolyl derivatives as PPAR activators
SI1734970T1 (sl) 2004-03-12 2015-04-30 Intercept Pharmaceuticals, Inc. Zdravljenje fibroze z uporabo FXR ligandov
US10987362B2 (en) 2004-03-12 2021-04-27 Intercept Pharmaceuticals, Inc. Treatment of fibrosis using FXR ligands
CN101048367A (zh) 2004-07-30 2007-10-03 萨尔瓦特实验室股份有限公司 作为PPARγ调节剂的新的酪氨酸衍生物
KR20070050475A (ko) * 2004-08-11 2007-05-15 교린 세이야꾸 가부시키 가이샤 신규 환상 아미노 안식향산 유도체
US7622491B2 (en) * 2004-08-13 2009-11-24 Metabolex Inc. Modulators of PPAR and methods of their preparation
PL371841A1 (pl) 2004-12-20 2006-06-26 ADAMED Sp.z o.o. Nowe związki pochodne kwasu 3-fenylopropionowego
PL372332A1 (pl) * 2005-01-19 2006-07-24 ADAMED Sp.z o.o. Nowe związki, pochodne kwasu 3-fenylopropionowego
PL372356A1 (pl) 2005-01-20 2006-07-24 ADAMED Sp.z o.o. Nowe związki, pochodne kwasu 3-fenylopropionowego
WO2006082495A1 (fr) * 2005-02-02 2006-08-10 Ranbaxy Laboratories Limited Modulateurs des recepteurs actives par les proliferateurs de peroxysomes
ITMI20050912A1 (it) 2005-05-19 2006-11-20 Erregierre Spa Processo di preparazione di acidi 3-a-ya(b)-diidrossi-6-a(b)-alchil-5b-colanici
WO2007023882A1 (fr) 2005-08-26 2007-03-01 Shionogi & Co., Ltd. Dérivé ayant une activité agoniste vis-à-vis du ppar
US8653115B2 (en) * 2006-06-13 2014-02-18 Shanghai Institute Of Materia Medica, Chinese Academy Of Sciences Heterocyclic non-nucleoside compounds, their preparation, pharmaceutical composition and their use as antiviral agents
MX2009002282A (es) 2006-09-07 2009-03-20 Nycomed Gmbh Tratamiento de combinacion para diabetes mellitius.
KR20090066289A (ko) 2006-09-08 2009-06-23 로드아일랜드하스피틀 알코올 유발성 뇌 질환의 치료, 예방 및 역행
EP2112995B1 (fr) 2007-01-19 2013-07-31 Intercept Pharmaceuticals, Inc. Acides biliares substitues en 23 utiles comme modulateurs de tgr5 et leurs methodes d'utilisation
JP2008239616A (ja) * 2007-02-28 2008-10-09 Iyaku Bunshi Sekkei Kenkyusho:Kk Hdl上昇剤
WO2008117982A1 (fr) * 2007-03-28 2008-10-02 Crystal Genomics, Inc. Dérivés d'acide carboxylique hétérocyclique et composition pharmaceutique les contenant pour inhiber l'accumulation des lipides
US20160331729A9 (en) 2007-04-11 2016-11-17 Omeros Corporation Compositions and methods for prophylaxis and treatment of addictions
US11241420B2 (en) 2007-04-11 2022-02-08 Omeros Corporation Compositions and methods for prophylaxis and treatment of addictions
AU2008240158B2 (en) 2007-04-11 2014-07-10 Omeros Corporation Compositions and methods for prophylaxis and treatment of addictions
JPWO2008139879A1 (ja) * 2007-04-26 2010-07-29 ファルマフロンティア株式会社 G蛋白質共役型レセプター抑制剤および医薬
EA021544B1 (ru) 2007-06-04 2015-07-30 Бен-Гурион Юниверсити Оф Дзе Негев Рисерч Энд Дивелопмент Оторити Триарильные соединения и фармацевтические композиции, их содержащие
CN105037476B (zh) 2008-07-30 2018-06-12 英特塞普特医药品公司 Tgr5调节剂及其使用方法
EP2376519B1 (fr) 2008-11-19 2013-11-13 Intercept Pharmaceuticals, Inc. Modulateurs de tgr5 et leur procédé d'utilisation
WO2010105103A1 (fr) 2009-03-11 2010-09-16 Omeros Corporation Compositions et méthodes pour la prophylaxie et le traitement d'addictions
US8581001B2 (en) 2010-04-16 2013-11-12 Codman & Shurtleff Metformin-cysteine prodrug
US20130156720A1 (en) 2010-08-27 2013-06-20 Ironwood Pharmaceuticals, Inc. Compositions and methods for treating or preventing metabolic syndrome and related diseases and disorders
US20120094959A1 (en) 2010-10-19 2012-04-19 Bonnie Blazer-Yost Treatment of cystic diseases
US9982008B2 (en) 2012-06-19 2018-05-29 Intercept Pharmaceuticals, Inc. Preparation and uses of obeticholic acid
RU2695383C2 (ru) * 2012-06-19 2019-07-23 Синбиас Фарма АГ Производные бендамустина, родственные соединения и их медицинское применение для лечения рака
SG11201408501UA (en) 2012-06-19 2015-01-29 Intercept Pharmaceuticals Inc Preparation, uses and solid forms of obeticholic acid
WO2014184104A1 (fr) * 2013-05-17 2014-11-20 Boehringer Ingelheim International Gmbh Dérivés de pyrrolidine, leurs compositions pharmaceutiques et leurs utilisations
EA201690938A1 (ru) 2013-11-05 2016-11-30 Бен-Гурион Юниверсити Оф Дзе Негев Рисерч Энд Дивелопмент Оторити Соединения для лечения диабета и осложнений, возникающих из-за этого заболевания
WO2016071727A1 (fr) 2014-11-04 2016-05-12 INSERM (Institut National de la Santé et de la Recherche Médicale) Méthodes pour la prévention et le traitement de la glomérulonéphrite rapidement progressive
US9987255B2 (en) 2014-12-19 2018-06-05 Merck Sharp & Dohme Corp. 5,5-bicyclic oxazole orexin receptor antagonists
CN104744282A (zh) * 2015-02-17 2015-07-01 南通恒盛精细化工有限公司 一种胰岛素增敏剂的制备工艺
WO2019224393A1 (fr) * 2018-05-25 2019-11-28 University Of Copenhagen Fénofibrate pour réduire l'hypoglycémie dans le lada/diabète de type 1

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5522636A (en) 1978-08-04 1980-02-18 Takeda Chem Ind Ltd Thiazoliding derivative
US4342771A (en) 1981-01-02 1982-08-03 Pfizer Inc. Hypoglycemic 5-substituted oxazolidine-2,4-diones
US4367234A (en) 1980-07-28 1983-01-04 Pfizer Inc. Hypoglycemic 5-substituted oxazolidine-2,4-diones
RU1473300C (ru) 1987-06-01 1995-02-09 Научно-производственное объединение "Витамины" Способ получения 4-бензоиламино-3-оксотетрагидротиофена
US5220023A (en) 1989-07-18 1993-06-15 Janssen Pharmaceutica N.V. Glycine derivatives
DE3941438A1 (de) 1989-12-15 1991-06-20 Hoechst Ag Neue 2-substituierte 4-(3-alkyl-5-tert.-butyl-4-hydroxy-phenyl)-thiazole, verfahren zu ihrer herstellung, die sie enthaltenden arzneimittel und ihre verwendung
US5089514A (en) * 1990-06-14 1992-02-18 Pfizer Inc. 3-coxazolyl [phenyl, chromanyl or benzofuranyl]-2-hydroxypropionic acid derivatives and analogs as hypoglycemic agents
WO1993021166A1 (fr) 1992-04-10 1993-10-28 Smithkline Beecham Plc Composes heterocycliques et leur utilisation pour le traitement du diabete du type ii
WO1994001420A1 (fr) 1992-07-03 1994-01-20 Smithkline Beecham Plc Composes heterocycliques comme produits pharmaceutiques
US5232945A (en) 1992-07-20 1993-08-03 Pfizer Inc. 3-aryl-2-hydroxypropionic acid derivatives and analogs as antihypertensives
GB9225386D0 (en) 1992-12-04 1993-01-27 Smithkline Beecham Plc Novel compounds
NZ262941A (en) 1993-03-29 1997-07-27 Zeneca Ltd Pyridine derivatives and medicaments
GB9311644D0 (en) 1993-06-05 1993-07-21 Smithkline Beecham Plc Novel compounds
GB9311661D0 (en) * 1993-06-05 1993-07-21 Smithkline Beecham Plc Novel compounds
SE9302332D0 (sv) 1993-07-06 1993-07-06 Ab Astra New compounds
GB9315148D0 (en) 1993-07-22 1993-09-08 Smithkline Beecham Plc Novel compounds
JPH08325263A (ja) * 1995-05-31 1996-12-10 Sumitomo Metal Ind Ltd 新規2−アミノ−3−フェニルプロピオン酸誘導体
JPH08325264A (ja) * 1995-05-31 1996-12-10 Sumitomo Metal Ind Ltd 新規2−芳香環置換−3−フェニルプロピオン酸またはアクリル酸誘導体
JPH08325564A (ja) 1995-06-05 1996-12-10 Nec Corp 有機薄膜el素子
CA2259487A1 (fr) * 1996-07-01 1998-01-08 Margaret Mary Faul Composes hypoglycemiants et hypolipidemiants

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BG102792A (bg) 1999-08-31
EA001403B1 (ru) 2001-02-26
ATE205485T1 (de) 2001-09-15
PT888317E (pt) 2002-03-28
NZ331381A (en) 2000-06-23
JP3255930B2 (ja) 2002-02-12
NO983940D0 (no) 1998-08-27
DK0888317T3 (da) 2002-01-21
AP9700935A0 (en) 1997-04-30
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IS1869B (is) 2003-05-09
IL125796A0 (en) 1999-04-11
RS49586B (sr) 2007-04-10
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US6294580B1 (en) 2001-09-25
EP0888317B1 (fr) 2001-09-12
BR9707786B1 (pt) 2009-12-01
SK116398A3 (en) 1999-04-13
AP780A (en) 1999-11-22
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EA199800664A1 (ru) 1999-04-29
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WO1997031907A1 (fr) 1997-09-04
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